用非临床模型评估透明质酸、硫酸软骨素和氯化钙的联合作用机制:HA+CS+CaCl2 溶液对三维人体重建膀胱上皮细胞的作用机制。

IF 1.3 Q4 ENGINEERING, BIOMEDICAL Medical Devices-Evidence and Research Pub Date : 2024-01-30 eCollection Date: 2024-01-01 DOI:10.2147/MDER.S433261
Laura Brambilla, Valeria Frangione, Marisa Meloni
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引用次数: 0

摘要

目的:《医疗器械法规》(欧盟)2017/745 要求通过实验数据证明主要作用模式(MoA)。Ialuril® Prefill(HA+CS+CaCl2组合:透明质酸钠1.6%、硫酸软骨素钠2% w/v和氯化钙0.87%)为III类医疗器械,适用于膀胱内灌注以减少尿路感染:三种实验设计:i) 挑选大肠杆菌菌株(DSM 103538 和 DSM 1103),研究 HA+CS+CaCl2 在 80%、50% 和 25% 浓度下改变液体肉汤中细菌生长(4 小时和 24 小时 CFU)的特性;ii) 通过量化咖啡因在上皮细胞中的渗透,评估暴露 15 分钟后在 HBE 上成膜的特性;iii) 对抗大肠杆菌粘附和生物膜的能力。iii) 以环丙沙星作为抗菌分子参照物,通过存活计数和扫描电子显微镜(SEM)进行超微结构分析,评估咖啡因在定植的 HBE 上抑制大肠杆菌粘附和生物膜形成的能力:结果:两种大肠杆菌菌株的细菌活力无明显差异。在 1 小时和 2 小时内,HA+CS+CaCl2 对咖啡因的渗透率分别降低了 51.7% 和 38.1%,这两个时间点的咖啡因渗透率均显著降低,证明 HA+CS+CaCl2 能够牢牢粘附在膀胱上皮细胞上,在表面形成物理屏障。经 HBE 处理的组织在感染大肠杆菌后的存活计数与阴性对照组没有差异,表明该装置没有抑制大肠杆菌的生长。扫描电子显微镜图像显示产品在 HBE 表面分布均匀,证实 HA+CS+CaCl2 能够粘附在膀胱上皮细胞上,抵消生物膜的形成:结论:研究结果表明,HA+CS+CaCl2 可通过物理机械作用模式抵御细菌入侵:这种医疗器械是治疗复发性尿道炎的抗生素有效替代品。
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Non Clinical Model to Assess the Mechanism of Action of a Combined Hyaluronic Acid, Chondroitin Sulfate and Calcium Chloride: HA+CS+CaCl2 Solution on a 3D Human Reconstructed Bladder Epithelium.

Purpose: Medical Device Regulation (EU) 2017/745 requires the principal mode of action (MoA) to be demonstrated by experimental data. The MoA of Ialuril® Prefill (combined as HA+CS+CaCl2: sodium hyaluronate 1.6%, sodium chondroitin sulphate 2% w/v and calcium chloride 0.87%) Class III medical device, indicated for intravesical instillation to reduce urinary tract infections, has been evaluated on a 3D reconstructed human bladder epithelium (HBE).

Methods: Three experimental designs; i) E. coli strain selection (DSM 103538, DSM 1103) to investigate the HA+CS+CaCl2 properties in modifying bacterial growth in liquid broth (CFU 4h and 24h) at 80%, 50% and 25% concentrations; ii) evaluation of film forming properties on HBE after 15 min exposure by quantifying caffeine permeation across the epithelium; iii) capacity to counteract E. coli adhesion and biofilm formation on colonized HBE by viable counts and ultrastructural analysis by scanning electron microscopy (SEM) using ciprofloxacin as the reference antimicrobial molecule.

Results: No significant differences were observed in bacterial viability for both the E. coli strains. HA+CS+CaCl2 reduced caffeine permeation of 51.7% and 38.1% at 1h and 2h, respectively and determined a significant decrease in caffeine permeation rate at both timepoints supporting HA+CS+CaCl2 capacity to firmly adhere to the bladder epithelium creating a physical barrier on the surface. The viable counts in HBE treated tissues then infected with E. coli resulted not different from the negative control suggesting that the device did not inhibit E. coli growth. SEM images showed homogenous product distribution over the HBE surface and confirmed the capacity of HA+CS+CaCl2 to adhere to the bladder epithelium, counteracting biofilm formation.

Conclusion: The results support the capacity of HA+CS+CaCl2 to counteract bacterial invasion by using a physico-mechanical mode of action: this medical device represents a valid alternative to antibiotics in the treatment of recurrent UTIs.

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来源期刊
Medical Devices-Evidence and Research
Medical Devices-Evidence and Research ENGINEERING, BIOMEDICAL-
CiteScore
2.80
自引率
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发文量
41
审稿时长
16 weeks
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